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A.M.I. HAL Knotpusher

by A.M.I. Agency for Medical Innovations GmbH United States EUDAMED

Ref AHK 007

EMDN L0299

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EAMIA34B9C1D1N8 Basic UDI-DIDate29 Aug 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Trilogy Intruments
Model / Reference
AHK 007
Primary DI / UDI-DI
+EAMIAHK0070
Basic UDI-DI
++EAMIA34B9C1D1N8
Direct Marketing DI
+EAMIAHK0070
EMDN Code
L0299 Suture instruments, reusable - other
Device Class
Class I
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
AT-MF-000016792

Other devices from A.M.I. Agency for Medical Innovations GmbH

See all devices from A.M.I. Agency for Medical Innovations GmbH →

Properties & raw data

Show properties, registry sources and raw records
  • Reusable
Other properties (12)
  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED be322a0c-094f-496c-a726-4f5a4663fce7 61 fields · synced 22 Oct 2026